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Figure 2 | Biotechnology for Biofuels

Figure 2

From: Development of a fluorescence-based method for monitoring glucose catabolism and its potential use in a biomass hydrolysis assay

Figure 2

Sensitivity and dynamic range. E. coli strain crp*-gfp grown in modified 1 × M9 minimal media for 20 h with increasing amounts of glucose. (a) Each time point is the average absorbance of four replications of each E. coli strain. (b) Each time point is the average fluorescence of four replications of crp*-gfp cultures minus the average fluorescence of four replications of crp*-gfp- cultures. All points are the mean ± s.e.

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